Uno studio per scoprire quanto sia sicura la darolutamide e come funzioni in combinazione con la terapia di deprivazione androgenica e docetaxel nell'assistenza medica di routine per uomini giapponesi affetti da cancro alla prostata metastatico sensibile agli ormoni a basso volume (HAYATE)
Uno studio osservazionale su darolutamide in aggiunta alla terapia standard di deprivazione androgenica e docetaxel in pazienti con carcinoma della prostata metastatico sensibile agli ormoni a basso volume
This is an observational study in which medical records of Japanese men with low-volume metastatic hormone-sensitive prostate cancer (mHSPC), who received treatment with a combination therapy of darolutamide with an androgen deprivation therapy (ADT) and docetaxel, will be collected and studied.
The study drug darolutamide, in combination with ADT and docetaxel is an approved treatment for another type of prostate cancer. To better understand the impact of this combination therapy on low-volume mHSPC and make better treatment choices, more knowledge is needed. ADT is a hormone therapy that lowers the level of testosterone, a male hormone, and slows down the growth of cancer cells. Darolutamide blocks androgen signals to slow the growth of the cancer cells. Docetaxel is a type of chemotherapy used to treat different types of cancer. It works by stopping the growth and spread of cancer cells.
The prostate gland is a male reproductive gland found below the bladder. Low-volume mHSPC is a cancer of the prostate gland that has spread beyond the gland to three or fewer bones but has not reached organs like the lungs and liver. The prostate cancer is considered hormone sensitive when it responds to an anti hormonal therapy.
In this study, only observations from routine clinical practices will be made. Participants will receive darolutamide, in combination with ADT and docetaxel as prescribed by their doctors during routine medical care. The participants will not receive any advice on treatment or any changes to healthcare as a part of the study.
The main purpose of this study is to learn more about how safe darolutamide is and how well it works in combination with ADT and docetaxel in adult Japanese men with mHSPC in routine medical care.
To do this, researchers will assess the following information about participants after one year of receiving the combination therapy by their doctors:
• the number of participants who achieve normal levels of prostate specific antigen (PSA).
PSA is a protein found in the blood that helps doctors monitor prostate cancer.
• the number of participants who have adverse events (AEs), serious adverse events (SAEs), and adverse events of special Interest (AESIs) that lead to discontinuation or change in the dose of darolutamide or docetaxel during the study.
AEs are medical problems that the participants had during the study that may or may not be related to the study treatment.
SAEs are AEs that lead to death, puts the participant's life at risk, requires hospitalization, causes disability, causes a baby to be born with medical problems, or is medically important.
AESIs are specific medical problems the participants had during the study that may be related to heart, lung, liver etc.
The data will come from the participant's medical records and will be collected between October 2024 and June 2031. Researchers will only look at the health records from adult men with mHSPC in Japan. No separate visits are required as part of the study. The participants will only visit their doctor at the study clinic as part of their routine medical care.
Panoramica dello studio
Stato
Intervento / Trattamento
Tipo di studio
Iscrizione (Stimato)
Contatti e Sedi
Contatto studio
- Nome: Bayer Clinical Trials Contact
- Numero di telefono: 0018888422937
- Email: clinical-trials-contact@bayer.com
Luoghi di studio
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Multiple Locations, Giappone
- Reclutamento
- Many locations
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-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Metodo di campionamento
Popolazione di studio
Male patients over the age of 18 years with a diagnosis of low-volume metastasis HSPC whom the decision for treatment with darolutamide in combination with docetaxel and ADT has been made by the physician or a delegate.
Descrizione
Inclusion Criteria:
- Histologically or cytologically confirmed adenocarcinoma of prostate.
- Patients have low-volume of metastatic disease documented by either by a positive bone scan, or for soft tissue either by contrast-enhanced abdominal/pelvic/chest computed tomography (CT) or magnetic resonance imaging (MRI) scan assessed by investigator. Low-volume metastasis criteria is defined as "not" meeting the high-volume criteria of the CHAARTED trial; high-volume meet the presence of visceral metastases, or four or more bone lesions including at least one outside the vertebral column or pelvis.
- Documented diagnosis of mHSPC.
- Patients on triplet regimen previously decided by the investigator irrespective of enrollment in the study.
- Start ADT within 6 months before or at the index date.
- Signed informed consent: If an eligible patient is deceased at the time of study initiation, informed consent from the legally representative(s) of the patient is required. Opt-out consent is acceptable in accordance with the Ethical Guidelines for Medical and Health Research Involving Human Subjects only when it is difficult to obtain signed informed consent from the patient or their legal representative.
Exclusion Criteria:
- Patients treated with docetaxel before darolutamide start.
- Participation in an investigational program with interventions outside of routine clinical practice.
- Contra-indications to darolutamide, docetaxel and ADT according to the local marketing authorization.
- Participation in the PASS of darolutamide in patients with mHSPC (DADOX [NCT06010914]).
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Modelli osservazionali: COHORT
- Prospettive temporali: PROSPECTIVE
Coorti e interventi
Gruppo / Coorte |
Intervento / Trattamento |
|---|---|
|
mHSPC patients
Adult male patients with a diagnosis of low-volume metastasis HSPC (hormone-sensitive prostate cancer) whom the decision for treatment with darolutamide in combination with docetaxel and ADT has been made by the physician or a delegate. |
Follow clinical practice/administration. ADT=androgen deprivation therapy. |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Proportion of patients with absolute prostate-specific antigen (PSA) response at 12 months
Lasso di tempo: after 12 months
|
Absolute PSA response is defined as blood PSA level <0.2 ng/mL during treatment period. Proportion of patients with absolute PSA response is defined as the number of patients with absolute PSA response, divided by the total number of patients evaluable for absolute PSA response. Proportion of patients with absolute PSA response will be evaluated on patient data up to 12 months after index date. |
after 12 months
|
|
Number of patients with adverse event of special interests (AESIs), serious adverse events (SAEs) and adverse events (AEs) leading to dose modification or discontinuation of darolutamide or docetaxel at 12 months
Lasso di tempo: after 12 months
|
AESIs are defined as: Cardiac disease, Interstitial lung disease, Liver dysfunction, Neutropenia, Febrile neutropenia, Thrombocytopenia, Hypertension, Anemia, Hyperglycemia, Urinary tract infection, Decreased appetite, Fatigue, Nausea, Peripheral neuropathy, Dysgeusia. |
after 12 months
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Tempo reale per il cancro alla prostata resistente alla castrazione (CRPC)
Lasso di tempo: fino a 12 mesi
|
fino a 12 mesi
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Tempo all’inizio della successiva terapia antineoplastica sistemica
Lasso di tempo: fino a 12 mesi
|
fino a 12 mesi
|
|
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Tempo all'inizio dell'uso di oppioidi per ≥7 giorni consecutivi in pazienti che al basale erano liberi da oppioidi
Lasso di tempo: fino a 12 mesi
|
fino a 12 mesi
|
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Real-world time to PSA progression in patients who have a documentation of PSA
Lasso di tempo: up to 12 months
|
PSA progression is defined as a ≥ 25% PSA increase above the nadir value and an increase in absolute value of ≥2 ng/mL above nadir. The time to PSA progression is defined as the time from index date to the date of first PSA progression. |
up to 12 months
|
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Time to first symptomatic skeletal event (SSE)
Lasso di tempo: up to 12 months
|
An SSE is defined as external beam radiation therapy (EBRT) to relieve skeletal symptoms, or new symptomatic pathologic bone fracture, or occurrence of spinal cord compression or tumor-related orthopedic surgical intervention, whichever comes first. |
up to 12 months
|
|
Dosing patterns of darolutamide and docetaxel up to 12 months
Lasso di tempo: after 12 months
|
The darolutamide and docetaxel administration patterns will be summarized as dosage (initial, overall), duration of administration, number of cycles administered (docetaxel only), dose modification, relative dose intensity (RDI), reason of dose modification or discontinuation. |
after 12 months
|
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Summary description of patient demographics / characteristics
Lasso di tempo: after 12 months
|
Age at baseline, Age category, Race (Japanese or not), Physical examination including height and weight, Body Mass Index (BMI), BMI category, Comorbidities (Cardiac disease, Lung disease, Liver dysfunction, etc.), ECOG PS (Eastern Cooperative Oncology Group Performance Status), and other medical history. |
after 12 months
|
|
Summary description of laboratory values
Lasso di tempo: after 12 months
|
Descriptive statistics (i.e. number of observations) will be presented for the laboratory values, their changes from baseline (including baseline value), and their percent changes from baseline. |
after 12 months
|
Collaboratori e investigatori
Sponsor
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Effetti fisiologici dei farmaci
- Ormoni, sostituti ormonali e antagonisti ormonali
- Antagonisti ormonali
- Prodotti chimici organici
- Azioni farmacologiche
- Azioni e usi chimici
- Idrocarburi
- Cicloparaffins
- Idrocarburi, aliciclici
- Idrocarburi, ciclici
- Terpeni
- Taxoidi
- Ciclodecani
- Diterpenes
- Docetaxel
- Antagonisti degli androgeni
- Daroutamide
Altri numeri di identificazione dello studio
- 22842
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Descrizione del piano IPD
Availability of this study's data will later be determined according to Bayer's commitment to the EFPIA/PhRMA "Principles for responsible clinical trial data sharing". This pertains to scope, timepoint and process of data access. As such, Bayer commits to sharing upon request from qualified researchers patient-level clinical trial data, study-level clinical trial data, and protocols from clinical trials in patients for medicines and indications approved in the US and EU as necessary for conducting legitimate research. This applies to data on new medicines and indications that have been approved by the EU and US regulatory agencies on or after January 01, 2014. Interested researchers can use www.vivli.org to request access to anonymized patient-level data and supporting documents from clinical studies to conduct research. Information on the Bayer criteria for listing studies and other relevant information is provided in the member section of the portal.
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .